Clinical Trials Directory

Trials / Completed

CompletedNCT01859715

Emergency Department (ED) Drug Interaction in Emergency Department Patients

Hepatic Cytochrome Drug Interactions in Emergency Department Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
502 (actual)
Sponsor
University of Colorado, Denver · Academic / Other
Sex
All
Age
18 Years – 95 Years
Healthy volunteers
Not accepted

Summary

This study examines how hepatic cytochrome CYP2D6 drug interactions affects the efficacy of oxycodone, hydrocodone, and ondansetron in Emergency Department (ED) patients.

Detailed description

Patients with pain and/or nausea are enrolled in the Emergency Department (ED). They are given either oxycodone, hydrocodone, or ondansetron at the discretion of the Emergency Department (ED) provider or the triage nurse by triage protocol. Detailed prescription, over the counter, herbal, supplement, and illicit drug ingestion histories are taken from the patient or their health care proxy. Serial visual analogue scales are captured prior to study drug administration then between 30 and 90 minutes following drug administration.

Conditions

Interventions

TypeNameDescription
DRUGOxycodoneSubjects given oxycodone 5mg by ED provider decision or by triage nurse randomization.
DRUGHydrocodoneSubjects given hydrocodone/acetaminophen 5mg/500mg by ED provider decision or by triage nurse randomization.
DRUGOndansetronSubjects given ondansetron 4mg for reported nausea or vomiting. Treatment determined either by triage nursing protocol or by provider discretion. Observational intervention only.

Timeline

Start date
2012-06-01
Primary completion
2013-01-01
Completion
2013-02-01
First posted
2013-05-22
Last updated
2016-05-05
Results posted
2016-05-05

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01859715. Inclusion in this directory is not an endorsement.